Rapid Assembly of Polyfunctional Structures Using a One-Pot Five- and Six-Component Sequential Groebke-Blackburn/Ugi/Passerini Process

被引:57
作者
Al-Tel, Taleb H. [1 ,2 ]
Al-Qawasmeh, Raed A. [3 ]
Voelter, Wolfgang [4 ]
机构
[1] Univ Sharjah, Coll Pharm, Sharjah, U Arab Emirates
[2] Univ Sharjah, Sharjah Inst Med Res, Canc Div, Sharjah 27272, U Arab Emirates
[3] Univ Jordan, Dept Chem, Amman 11942, Jordan
[4] Univ Tubingen, Interfak Inst Biochem, D-72076 Tubingen, Germany
关键词
Multicomponent reactions; Heterocycles; Drug discovery; Cycloaddition; Molecular diversity; DIVERSITY-ORIENTED SYNTHESIS; MULTICOMPONENT REACTIONS; COMBINATORIAL SYNTHESIS; 3-COMPONENT REACTION; ISOCYANIDES; CHALLENGE; ALDEHYDES; PYRAZINES; CHEMISTRY;
D O I
10.1002/ejoc.201000808
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Sequential addition of up to six components under well-defined conditions results in the formation of novel structures with amino acid, peptide, and heterocyclic components. This process forms up to eight new bonds under very mild conditions and tolerates a broad spectrum of functional groups. An orthogonal union of the Groebke-Blackburn three-component reaction with the Ugi four-component or Passerini three component reaction was adopted to synthesize polyfunctionalized heterocycles. In terms of diversity oriented synthesis, 10 positions on the basic polycyclic structure can be varied. Straightforward batch splitting provides a simple and efficient method for preparing structurally complex analogs.
引用
收藏
页码:5586 / 5593
页数:8
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